Canonical Allele Identifier: PA2825121972
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2888353
ClinVar RCV Id: RCV003610784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Asn1112Lys
CA374111873
NM_000264.5:c.3336C>A
CA374111874
NM_000264.5:c.3336C>G