Canonical Allele Identifier: PA2825490411
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.Met1056Lys
CA196571104
NM_001083602.3:c.3167T>A