Canonical Allele Identifier: PA2825122011
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Met1122Val
CA374111821
NM_000264.5:c.3364A>G