Canonical Allele Identifier: PA2825119177
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2911465
ClinVar RCV Id: RCV003609785
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Thr211Ser
CA374115060
NM_000264.5:c.631A>T